smelling salts

Manufacturer
Shenzhen Ze'ai Electronic Co., Ltd.
Effective date
2025-09-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:13:28

Label at a glance#

Productsmelling salts
Active ingredientAMMONIA
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ammonia 15%

OTC - PURPOSE SECTION

Inhalant

INDICATIONS & USAGE SECTION

For the temporarystimulation ofthe senses to restore alertness.

WARNINGS SECTION

For inHalAtion use only.
Avoid direct contact with eyes.lfcontact occurs,rinse thoroughly with water fori5 minutes.Use only as directed. Misuse may be harmful.
Use in a well-ventilated area.Do notuse in enclosedspaces
Prolonged exposure maycause irritation.Discantinue useifdiscomfort occurs.
Possible side effectsinclude nasallritation,coughing.or shortness of breath.lfsymptoms persist, discontinue use and consulta doctor

OTC - DO NOT USE SECTION

Do not ingest or apply to skin.

OTC - WHEN USING SECTION

Avoid contact with eyes,ears, and mouth.

Ifproduct gets into eyes, rinse thoroughly with water for 15minutes.
Stop use and ask a doctorifirritation orrash occurs.
These may be signs ofaserious condition.

OTC - STOP USE SECTION


Stop use and ask a doctorifirritation or rash occurs.
These may be signs ofa serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


Keep outofreach ofchildren.lfswallowed,get medical
help or contacta Poison control center immediately at 1-800-222-1222.

INACTIVE INGREDIENT SECTION

Alcohol
Cotton
Peppermint Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1299889ammonia 15 % Nasal InhalantPSN4
1299889ammonia 150 MG/ML Nasal InhalantSCD4
1299889ammonia 0.045 GM per 0.3 ML Nasal InhalantSY4
1299889ammonia 0.3 ML Nasal InhalantSY4
1299889ammonia 15 % Nasal InhalantSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85765-002-01smelling salts1 in 1 BOXPOWDER14
85765-002-01smelling salts53 g in 1 BOTTLEPOWDER534

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85765-00285765-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEPPERMINT OILAV092KU4JHIACT
AMMONIA5138Q19F1XACTIB
COTTON70LDW53ROOIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3e7d9eff-dd7a-668e-e063-6394a90a404f38601f38-09ef-9bb2-e063-6294a90a83d62025-09-10WarningsExact identifier
spl id: 3e7d9eff-dd7a-668e-e063-6394a90a404f
spl set id: 38601f38-09ef-9bb2-e063-6294a90a83d6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.